Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2400-2026 — Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

U.S. FDA — Device Enforcement · United States · 2026-05-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2400-2026
Date of alert
2026-05-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Inter-Med Llc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00371347008104
Reported risk: Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.